RecallHawk

Ferrous Sulfate (Iron) Enteric-Coated Tablets, 324 mg - 100 Tablet Bottles

Prodigy Innovation LLC, of Princeton, New Jersey

Summary

CPSC recall: Ferrous Sulfate (Iron) Enteric-Coated Tablets, 324 mg - 100 Tablet Bottles. By Prodigy Innovation LLC, of Princeton, New Jersey. Hazard: The recalled dietary supplements contain iron which must be in child-resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.. Remedy: Consumers should immediately store the recalled dietary supplem

Details

Source

CPSC Consumer Product Recall

External ID

9652

Action Date

2023-06-22

Status

Recalled

Category

consumer_product

Product Description

This recall involves Ferrous Sulfate Enteric-Coated Tablets dietary supplements containing 324 mg of ferrous sulfate (ir

Context & Analysis

This is a unclassified recall.

This was one of 10 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Prodigy Innovation LLC, of Princeton, New Jersey has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Prodigy Innovation LLC, of Princeton, New Jersey) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Prodigy Innovation LLC, of Princeton, New Jersey have FDA actions?

Prodigy Innovation LLC, of Princeton, New Jersey has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9652" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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